GVAX in Advanced Prostate Cancer Patients Made Lymphopenic

Status unconfirmed · Phase 1/Phase 2

Conditions studied: Prostate Cancer

In brief

Androgen (a male sex hormone) deprivation is the standard therapy for metastatic prostate cancer and results in regression or control of disease in 80-85% of patients. This hormone therapy results in a progression-free survival of 12-18 months and overall survival of 24-30 months. However, all patients ultimately develop hormone-refractory prostate cancer (HRPC). Management of HRPC patients is a significant challenge for both patient and physician. Neither past nor current chemotherapy regimens have shown curative potential in patients with HRPC. Thus new treatment strategies are a high priority. A major focus of new treatment strategies is to enlist the aid of the immune system, particularly the development of prostate cancer vaccines. There has been a number of studies using dendritic cell based vaccines and the treatment has been well tolerated. Specific T-cell immune responses have been observed and occasional evidence for tumor regression. A reduction in serum prostate-specific antigen (PSA) has been observed as well. Lengthening the time-to-progression and delays in the onset of bone pain have been observed in subsets of patients with HRPC. The initial preclinical observations suggesting that a granulocyte-macrophage colony-stimulating factor (GM-CSF) gene transduced allogeneic (GVAX) prostate cancer vaccine may be efficacious in poorly immunogenic cancers were reported. The objective of this study is to evaluate the safety and immunologic effects of vaccinations with Allogeneic Prostate GVAX® (CG1940 \& CG8711) in patients made lymphopenic by treatment with chemotherapy and infused with autologous peripheral blood mononuclear cells (PBMC). Clinical observations and laboratory measurements will be monitored to evaluate safety, toxicity and immune responses. Additionally, the effects of treatment on serum PSA levels and tumor response will be evaluated.

Key facts

Study ID

NCT00122005

Run by

Providence Health & Services

People needed

18

Starts

2005-07-01

Expected to finish

2005-07-01

Last updated by the study team

2009-02-24

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Histologically diagnosed adenocarcinoma of the prostate
• Progressive disease
• ECOG performance status of 0 or 1
• Adequate bone marrow, renal and hepatic function
• Castrate levels of testosterone
• May have had local radiotherapy as part of their initial treatment or 28 days after palliative radiotherapy or one chemotherapy treatment for metastatic disease

You may not qualify if…

• Transitional cell, small cell or squamous cell prostate cancer
• Systemic steroid therapy within 10-days of enrollment
• Documented history of active autoimmune disease such as lupus, sarcoidosis, rheumatoid arthritis, glomerulonephritis or vasculitis
• Clinically significant active infections
• History of other malignancies over past 5-years (except non-melanoma skin cancer or controlled superficial bladder cancer)
• Uncontrolled medical problems (i.e. neurological, cardiovascular) considered high risk for investigational new drug treatment
• Prior treatment with an investigational drug within 30-days of study entry
• Seropositive for HIV, hepatitis B surface antigen or hepatitis C

Where it is running

• Providence Portland Medical Center — Portland, Oregon, United States

Full record on ClinicalTrials.gov

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